Results 41 to 50 of about 56,696 (118)

Cutaneous periumbilical purpura in disseminated strongyloidiasis in cancer patients: a pathognomonic feature of potentially lethal disease?

Brazilian Journal of Infectious Diseases
Cutaneous manifestations in disseminated strongyloidiasis are infrequent but should raise the suspicion for its diagnosis. We retrospectively evaluated the charts of six patients with cancer and a proven diagnosis of disseminated strongyloidiasis.
Jorge I. F. Salluh, Fernando A. Bozza, Tatiana S. Pinto, Luisa Toscano, Peter F. Weller, Marcio Soares   +5 more
doaj   +1 more source

Invasive Meningococcal Disease in a Patient With Complement 7 Deficiency

Journal of General and Family Medicine
Neisseria meningitidis can cause invasive meningococcal disease (IMD). Individuals with primary complement deficiencies are at a higher risk of developing IMD. However, cases of IMD associated with complement deficiency have rarely been reported in Japan.
Hiroaki Nishioka, Kazuki Maegawa, Shigeo Hara   +2 more
doaj   +1 more source

Purpura as the initial manifestation of IgG4-related disease with concomitant systemic lupus erythematosus: a case report

Frontiers in Medicine
Purpura is a common clinical manifestation of a wide variety of diseases, including extremely uncommon conditions. In this study, we report the case of a 61-year-old man who initially presented with purpura and was ultimately diagnosed with coexisting ...
Yi Wei, Yi Wei, Fuhua Chen, Ruomeng Li, Zhen Zhao, Yajuan Huang   +5 more
doaj   +1 more source

Acute immune thrombocytopenic purpura triggered by insect bite

Journal of Indian Society of Pedodontics and Preventive Dentistry, 2009
Idiopathic Thrombocytopenic Purpura (ITP) is a blood disorder characterized by an abnormal decrease in the number of platelets in the blood. Acute thrombocytopenic purpura is most commonly seen in young children, with a sudden onset, following a viral ...
Namdev R, Dutta S, Singh H
doaj  

Eosinophilic granulomatosis with polyangiitis developed during treatment with benralizmab for severe asthma: A case report and literature review

Respirology Case Reports
Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare autoimmune disorder characterized by necrotizing vasculitis, asthma, and eosinophilia. We report a case of EGPA that developed during benralizumab treatment for severe asthma and provide a ...
Mitsukuni Sakabe, Kazunori Tobino, Yumi Obata, Shota Sogabe, Kazuki Uchida, Yosuke Murakami   +5 more
doaj   +1 more source

A Case Report of Acute Hemorrhagic Edema of Infancy

پزشکی بالینی ابن سینا, 2005
Introduction: Acute hemorrhagic edema of infancy is an acute and rare cutaneous disorder that affects children between 4 months to 2 years of age and characterized by cutaneous purpuric lesions with millimeters to centimeters diameter.
Mozhgan Safari, Hasan Bazmamoun, Hesamoddin Nabavizadeh   +2 more
doaj  

Purpura Fulminans Mimicking NSTI: A Limb-saving case of <i>Haemophilus influenzae</i> Infection. [PDF]

IDCases
Watanabe R, Kono A, Narita C, Miyake A, Tosaka N.   +4 more
europepmc   +1 more source

Distinct purpuric lesions in patients with dermatomyositis

JAAD Case Reports, 2021
Sung Kyung Cho, BA, Elizabeth Messenger, MD, David Franklin Fiorentino, MD, PhD   +2 more
doaj   +1 more source

Severe Thrombocytopenia With Wet Purpura in Brucellosis: A Case Report. [PDF]

Clin Case Rep
Ravanbakhsh Ghavghani F, Oskouei HO, Leylabadlo HE.   +2 more
europepmc   +1 more source

Mucocutaneous Manifestations of Primary Systemic Amyloidosis: A Descriptive Study from Eastern India. [PDF]

Indian Dermatol Online J
Ghosh SK, Panja S, Majumder B, Pramanik M.   +3 more
europepmc   +1 more source